Mutation

Primary Site >> Stomach Cancer

Gene >> MTOR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11212346:11212346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557533784
CDS Mutation	c.3527C>T
AA Mutation	p.Thr1176Met(p.T1176M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11243280:11243280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246A>G
AA Mutation	p.Thr416Ala(p.T416A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361445
Start	11144649:11144649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4871A>G
AA Mutation	p.Gln1624Arg(p.Q1624R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11230961:11230961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2743G>T
AA Mutation	p.Val915Phe(p.V915F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11124583:11124583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6577C>T
AA Mutation	p.Arg2193Cys(p.R2193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11247699:11247699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151A>G
AA Mutation	p.Lys384Arg(p.K384R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11209451:11209451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3662C>T
AA Mutation	p.Thr1221Ile(p.T1221I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11241663:11241663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431G>T
AA Mutation	p.Gln477His(p.Q477H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11230975:11230975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2729G>A
AA Mutation	p.Arg910Gln(p.R910Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11108220:11108220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7595C>T
AA Mutation	p.Ala2532Val(p.A2532V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11109318:11109318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7500T>G
AA Mutation	p.Ile2500Met(p.I2500M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11238594:11238594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1810C>T
AA Mutation	p.Arg604Cys(p.R604C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11253900:11253900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11253880:11253880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799A>G
AA Mutation	p.Ile267Val(p.I267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11240377:11240377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749766561
CDS Mutation	c.1712C>T
AA Mutation	p.Thr571Met(p.T571M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11238576:11238576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828T>G
AA Mutation	p.Phe610Val(p.F610V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361445
Start	11243114:11243114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412A>C
AA Mutation	p.Lys471Thr(p.K471T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11121299:11121299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6880A>G
AA Mutation	p.Thr2294Ala(p.T2294A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11144673:11144673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4847G>A
AA Mutation	p.Arg1616His(p.R1616H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11253871:11253871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Glu270Lys(p.E270K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11122115:11122115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6674A>G
AA Mutation	p.Tyr2225Cys(p.Y2225C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11144750:11144750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4770G>C
AA Mutation	p.Met1590Ile(p.M1590I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11231308:11231308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2641C>T
AA Mutation	p.Arg881Cys(p.R881C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11237887:11237887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2164A>G
AA Mutation	p.Asn722Asp(p.N722D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11243166:11243166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1360C>T
AA Mutation	p.Arg454Cys(p.R454C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11157177:11157177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4444C>T
AA Mutation	p.Arg1482Cys(p.R1482C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11228828:11228828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2870G>A
AA Mutation	p.Arg957Gln(p.R957Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000361445
Start	11248004:11248004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200901835
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361445
Start	11248094:11248094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841C>T
AA Mutation	p.Arg281Cys(p.R281C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11240523:11240523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369221365
CDS Mutation	c.1566C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11213531:11213531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147272284
CDS Mutation	c.3153G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11121360:11121360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6819G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11121288:11121288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763361130
CDS Mutation	c.6891C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11231417:11231417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2532G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11228731:11228731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2967C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361445
Start	11124509:11124509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6651G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361445
Start	11234178:11234178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2296delC
AA Mutation	p.Arg766AspfsTer11(p.R766Dfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000361445
Start	11144650:11144650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4870C>T
AA Mutation	p.Gln1624Ter(p.Q1624*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000361445
Start	11243148:11243148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378C>T
AA Mutation	p.Arg460Ter(p.R460*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000361445
Start	11210861:11210861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3607C>T
AA Mutation	p.Arg1203Ter(p.R1203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361445
Start	11213489:11213490(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3194dupG
AA Mutation	p.Glu1066Ter(p.E1066*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	42
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000361445
Start	11115469:11115469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7017-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript